Canonical Allele Identifier: CA624565444

Gene: WDR81

Linked Data

• ClinVar Variation Id: 1696176
• ClinVar RCV Id: RCV002266320
• dbSNP Id: rs1194329020
• gnomAD v2: 17-1629610-T-TA
• gnomAD v3: 17-1726316-T-TA
• gnomAD v4: 17-1726316-T-TA
• MyVariant Identifiers: chr17:g.1629610_1629611insA (hg19) ; chr17:g.1726316_1726317insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1726317dup , CM000679.2:g.1726317dup	GRCh38
NC_000017.10:g.1629611dup , CM000679.1:g.1629611dup	GRCh37
NC_000017.9:g.1576361dup	NCBI36
NG_032811.1:g.14795dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.1358dup MANE Select	ENSP00000386609.1:p.Tyr453Ter
ENST00000309182.9:c.-123-1673dup	ENSP00000312074.5:n.-123-1673dup
ENST00000409644.5:c.1358dup	ENSP00000386609.1:p.Tyr453Ter
ENST00000418841.5:c.-89+1531dup	ENSP00000395198.1:n.-89+1531dup
ENST00000419248.5:c.-15+1531dup	ENSP00000407845.1:n.-15+1531dup
ENST00000437219.6:c.59-4063dup	ENSP00000391074.2:n.59-4063dup
ENST00000446363.5:c.-308-4438dup	ENSP00000401560.1:n.-308-4438dup
ENST00000455636.5:c.59-4063dup	ENSP00000395226.1:n.59-4063dup
ENST00000468539.5:c.63-6008dup	ENSP00000460742.1:n.63-6008dup
ENST00000492901.1:n.88-4063dup
NM_001163673.1:c.59-4063dup	NP_001157145.1:n.59-4063dup
NM_001163809.1:c.1358dup	NP_001157281.1:p.Tyr453Ter
NM_001163811.1:c.-15+1531dup	NP_001157283.1:n.-15+1531dup
NM_152348.3:c.-123-1673dup	NP_689561.2:n.-123-1673dup
XM_005256454.2:c.1358dup	XP_005256511.1:p.Tyr453Ter
XM_011523650.1:c.1358dup	XP_011521952.1:p.Tyr453Ter
XM_011523651.1:c.-124+1531dup	XP_011521953.1:n.-124+1531dup
XR_933973.1:n.1502dup
XM_011523651.2:c.-124+1531dup	XP_011521953.1:n.-124+1531dup
XM_017024184.1:c.1358dup	XP_016879673.1:p.Tyr453Ter
XR_001752427.1:n.1510dup
XR_933973.2:n.1510dup
NM_001163809.2:c.1358dup MANE Select	NP_001157281.1:p.Tyr453Ter
NM_001163811.2:c.-15+1531dup	NP_001157283.1:n.-15+1531dup
NM_152348.4:c.-123-1673dup	NP_689561.2:n.-123-1673dup
NM_001163673.2:c.59-4063dup	NP_001157145.1:n.59-4063dup